2013Journal of Heterocyclic ChemistryRequires access

The Behavior of 2‐Substituted‐3‐hydroxyisoindolinones in the Reaction with sec‐Butyllithium

Andrzej Jóźwiak, Magdalena Ciechańska

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Abstract

This paper presents a dualistic behavior of 2‐substituted‐3‐hydroxyisoindolones in reactions with sec‐butyllithium (sec‐BuLi). 2‐tert‐Butyl‐3‐hydroxy‐2,3‐dihydro‐1H‐isoindol‐1‐one (1a) treated with sec‐BuLi undergoes metalation at position 7. On the other hand, the reaction between 3‐hydroxy‐2‐phenyl‐2,3‐dihydroxyisoindol‐1‐one (1j) and sec‐BuLi results in 3‐sec‐butyl‐2‐phenyl‐2,3‐dihydroisiondol‐1‐one (3j).

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What this paper is about

This paper presents a dualistic behavior of 2‐substituted‐3‐hydroxyisoindolones in reactions with sec‐butyllithium (sec‐BuLi). 2‐tert‐Butyl‐3‐hydroxy‐2,3‐dihydro‐1H‐isoindol‐1‐one (1a) treated with sec‐BuLi undergoes metalation at position 7. On the other hand, the reaction between 3‐hydroxy‐2‐phenyl‐2,3‐dihydroxyisoindol‐1‐one (1j) and sec‐BuLi results in 3‐sec‐butyl‐2‐phenyl‐2,3‐dihydroisiondol‐1‐one (3j).

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Available abstract

This paper presents a dualistic behavior of 2‐substituted‐3‐hydroxyisoindolones in reactions with sec‐butyllithium (sec‐BuLi). 2‐tert‐Butyl‐3‐hydroxy‐2,3‐dihydro‐1H‐isoindol‐1‐one (1a) treated with sec‐BuLi undergoes metalation at position 7. On the other hand, the reaction between 3‐hydroxy‐2‐phenyl‐2,3‐dihydroxyisoindol‐1‐one (1j) and sec‐BuLi results in 3‐sec‐butyl‐2‐phenyl‐2,3‐dihydroisiondol‐1‐one (3j).

Key concepts: Chemistry, Metalation, Butyllithium, Medicinal chemistry

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